Other dementias (SNOMED-CT) V1.4



Codelist metadata

Coding system

SNOMED CT

Coding system release

36.2.0

Organisation

University of Bristol

Codelist ID

bristol/other-dementias-snomed-ct-v13

Version ID

4218070e

Versions

About

No metadata has been provided for this codelist.


Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code term
101421000119107 Dementia due to Parkinson's disease
1089521000000106 Predominantly cortical dementia
1089581000000107 Predominantly cortical dementia
1148924004 Dementia due to deficiency of folic acid
1156761002 Progressive supranuclear palsy progressive non fluent aphasia
1163119007 Creutzfeldt Jakob disease following graft of dura
1186877003 Dementia due to vitamin E deficiency
1186879000 Dementia due to thiamine deficiency
1186881003 Dementia due to niacin deficiency
1186883000 Dementia due to nutritional deficiency disorder
1186887004 Dementia caused by manganese and/or manganese compound
1187004001 Chronic traumatic encephalopathy
1230018005 Corticobasal syndrome
1259066002 Disorder of autonomic nervous system due to senile dementia of Lewy body type
1259121008 Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea
1259123006 Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula
1259124000 Amyotrophic lateral sclerosis with frontotemporal dementia
1259469003 Dementia due to Gerstmann Straussler Scheinker syndrome
1259471003 Dementia due to Hashimoto encephalopathy
1259473000 Dementia due to fragile X syndrome
1259478009 Dementia due to familial Creutzfeldt-Jakob disease
1259480003 Dementia due to fatal familial insomnia
1259494002 Dementia due to leukodystrophy
1259496000 Dementia due to Lyme disease
1259501004 Dementia due to kuru
1259503001 Dementia due to iatrogenic Creutzfeldt-Jakob disease
1259511006 Dementia due to Wilson disease
1259513009 Dementia due to Whipple disease
1259517005 Dementia due to systemic lupus erythematosus
1259519008 Dementia due to subacute sclerosing panencephalitis
1259522005 Dementia due to variant Creutzfeldt-Jakob disease
1259524006 Dementia due to trypanosomiasis
1259529001 Dementia due to sporadic Creutzfeldt-Jakob disease
1259579003 Dementia due to Behcet syndrome
1259581001 Dementia due to celiac disease
1259586006 Dementia due to autoimmune encephalitis
1259661008 Dementia due to inflammatory disorder of musculoskeletal system
1259673008 Dementia due to neurofilament inclusion body disease
1259677009 Dementia due to multiple system atrophy
1259679007 Dementia due to atypical pantothenate kinase associated neurodegeneration
1259990004 Dementia due to classical pantothenate kinase associated neurodegeneration
12741002 AIDS with dementia
130121000119104 Dementia due to Rett's syndrome
135811000119107 Lewy body dementia with behavioral disturbance
155061007 Creutzfeldt-Jakob disease
191474008 Alcoholic dementia: [other] or [NOS]
191493005 Dementia caused by drug
192167008 [X]Dementia: [multi-infarct] or [predominantly cortical]
192173009 [X]Dementia in other diseases classified elsewhere
192174003 [X]Dementia in Pick's disease
192175002 [X]Dementia in Creutzfeldt-Jakob disease
192176001 [X]Dementia in Huntington's disease
192177005 [X]Dementia in Parkinson's disease
192178000 Acquired immune deficiency syndrome dementia complex
192808003 Lewy body disease
192818008 Cerebral degeneration due to Creutzfeldt-Jakob disease
198681000000106 [X]Lewy body dementia
214031000000108 [X]Lewy body dementia
21921000119103 Dementia co-occurrent and due to Pick's disease
230258005 Amyotrophic lateral sclerosis with dementia
230270009 Frontotemporal dementia
230271008 Pick's disease with Pick bodies
230272001 Pick's disease with Pick cells and no Pick bodies
230274000 Frontal lobe degeneration with motor neurone disease
230275004 Lewy body disease
230276003 Lewy body disease
230277007 Lewy body disease
230281007 Argyrophilic grain disease
230282000 Post-traumatic dementia
230288001 Semantic dementia
231463001 Alcoholic dementia NOS
268615009 Other alcoholic dementia
278857002 Dementia of frontal lobe type
281004 Dementia associated with alcoholism
304603007 Variant Creutzfeldt-Jakob disease
312991009 Senile dementia of the Lewy body type
414351000000102 [X]Dementia in Creutzfeldt-Jakob disease
414361000000104 [X]Dementia in Huntington's disease
421529006 Dementia with acquired immunodeficiency syndrome
425390006 Dementia associated with Parkinson's Disease
42769004 Diffuse Lewy body disease with spongiform cortical change
429458009 Dementia due to Creutzfeldt Jakob disease
442344002 Dementia due to Huntington chorea
455381000000102 [X]Dementia in Pick's disease
464291000000103 [X]Dementia in other diseases classified elsewhere
479161000000109 [X]Dementia in Parkinson's disease
51928006 General paresis - neurosyphilis
544871000000102 Other alcoholic dementia
62102009 AIDS with presenile dementia
62239001 Parkinson-dementia complex of Guam
671511000000100 Alcoholic dementia NOS
698624003 Dementia associated with cerebral lipidosis
698625002 Dementia associated with normal pressure hydrocephalus
698626001 Dementia associated with multiple sclerosis
698725008 Dementia associated with neurosyphilis
698726009 Dementia associated with viral encephalitis
698781002 Dementia associated with cerebral anoxia
702393003 Frontotemporal dementia with gene located on 3p11
702421006 Familial encephalopathy with neuroserpin inclusion bodies
702426001 GRN-related frontotemporal dementia
702429008 Frontotemporal dementia with parkinsonism-17
703544004 Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
713060000 Sporadic Creutzfeldt-Jakob disease
713488003 Presenile dementia co-occurrent with human immunodeficiency virus infection
713844000 Dementia co-occurrent with human immunodeficiency virus infection
715574002 Posterior cortical atrophy syndrome
715662009 Iatrogenic Jakob-Creutzfeldt disease
715737004 Parkinsonism co-occurrent with dementia of Guadeloupe
715807002 Familial Creutzfeldt-Jakob
716281000 Primary progressive non fluent aphasia
716667005 Right temporal atrophy variant frontotemporal dementia
716994006 Behavioral variant of frontotemporal dementia
721219005 Familial Alzheimer-like prion disease
722977005 Dementia co-occurrent and due to neurocysticercosis
722978000 Dementia caused by toxin
722979008 Dementia due to metabolic abnormality
722980006 Dementia due to chromosomal anomaly
733184002 Dementia caused by heavy metal exposure
733185001 Dementia following injury caused by exposure to ionizing radiation
733191004 Dementia due to chronic subdural hematoma
733193001 Dementia co-occurrent and due to progressive multifocal leukoencephalopathy
734076008 Diffuse large B-cell lymphoma associated with chronic inflammation
762350007 Dementia due to prion disease
762351006 Dementia due to and following injury of head
783161005 Familial dementia British type
783258000 Familial dementia Danish type
788898005 Dementia caused by volatile inhalant
788899002 Dementia due to pellagra
792004 Jakob-Creutzfeldt disease
80098002 Diffuse Lewy body disease
82351000119105 Altered behavior due to Pick's disease
82361000119107 Altered behavior in dementia due to Huntington chorea
82371000119101 Dementia due to multiple sclerosis with altered behavior
82959004 Dementia paralytica juvenilis
838276009 Amyotrophic lateral sclerosis, parkinsonism, dementia complex
840452004 Classical sporadic Creutzfeldt-Jakob disease
840464007 Dementia due to carbon monoxide poisoning
860826006 Creutzfeldt-Jakob Disease caused by human growth hormone
88520007 Creutzfeldt-Jakob agent
90194001 AIDS with organic dementia
922061000000103 Sporadic Creutzfeldt-Jakob disease
922071000000105 Sporadic Creutzfeldt Jakob disease

Codes not in the full codelist are in faint grey.